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Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial

dc.contributor.authorKeene, Keith L.
dc.contributor.authorChen, Wei-Min
dc.contributor.authorChen, Fang
dc.contributor.authorWilliams, Stephen R.
dc.contributor.authorElkhatib, Stacey D.
dc.contributor.authorHsu, Fang-Chi
dc.contributor.authorMychaleckyj, Josyf C.
dc.contributor.authorDoheny, Kimberly F.
dc.contributor.authorPugh, Elizabeth W.
dc.contributor.authorLing, Hua
dc.contributor.authorLaurie, Cathy C.
dc.contributor.authorGogarten, Stephanie M.
dc.contributor.authorMadden, Ebony B.
dc.contributor.authorWorrall, Bradford B.
dc.contributor.authorSale, Michele M.
dc.date.accessioned2016-06-03T16:16:18Z
dc.date.available2016-06-03T16:16:18Z
dc.date.issued2014-08
dc.description.abstractBackground: B vitamins play an important role in homocysteine metabolism, with vitamin deficiencies resulting in increased levels of homocysteine and increased risk for stroke. We performed a genome-wide association study (GWAS) in 2,100 stroke patients from the Vitamin Intervention for Stroke Prevention (VISP) trial, a clinical trial designed to determine whether the daily intake of high-dose folic acid, vitamins B6, and B12 reduce recurrent cerebral infarction. Methods: Extensive quality control (QC) measures resulted in a total of 737,081 SNPs for analysis. Genome-wide association analyses for baseline quantitative measures of folate, Vitamins B12, and B6 were completed using linear regression approaches, implemented in PLINK. Results: Six associations met or exceeded genome-wide significance (P ≤ 5 × 10−08). For baseline Vitamin B12, the strongest association was observed with a non-synonymous SNP (nsSNP) located in the CUBN gene (P = 1.76 × 10−13). Two additional CUBN intronic SNPs demonstrated strong associations with B12 (P = 2.92 × 10−10 and 4.11 × 10−10), while a second nsSNP, located in the TCN1 gene, also reached genome-wide significance (P = 5.14 × 10−11). For baseline measures of Vitamin B6, we identified genome-wide significant associations for SNPs at the ALPL locus (rs1697421; P = 7.06 × 10−10 and rs1780316; P = 2.25 × 10−08). In addition to the six genome-wide significant associations, nine SNPs (two for Vitamin B6, six for Vitamin B12, and one for folate measures) provided suggestive evidence for association (P ≤ 10−07). Conclusion: Our GWAS study has identified six genome-wide significant associations, nine suggestive associations, and successfully replicated 5 of 16 SNPs previously reported to be associated with measures of B vitamins. The six genome-wide significant associations are located in gene regions that have shown previous associations with measures of B vitamins; however, four of the nine suggestive associations represent novel finding and warrant further investigation in additional populations.en_US
dc.identifier.citationFrontiers in Public Health; 2: p. 1-8en_US
dc.identifier.doi10.3389/fpubh.2014.00112
dc.identifier.issn2296-2565
dc.identifier.pmidpmc4123605en_US
dc.identifier.urihttp://hdl.handle.net/10342/5452
dc.relation.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4123605/en_US
dc.subjectVISPen_US
dc.subjectassociationen_US
dc.subjectGWASen_US
dc.subjectone-carbon metabolismen_US
dc.subjectB12en_US
dc.subjectB6en_US
dc.subjectfolateen_US
dc.titleGenetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trialen_US
dc.typeArticleen_US
ecu.journal.nameFrontiers in Public Healthen_US
ecu.journal.pages1-8en_US
ecu.journal.volume2en_US

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